Spectroscopy and formation of lanthanum-hydrocarbon radicals formed by association and carbon-carbon bond cleavage of isoprene

被引:0
|
作者
Cao, Wenjin [1 ]
Hewage, Dilrukshi [1 ]
Yang, Dong-Sheng [1 ]
机构
[1] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2018年 / 148卷 / 19期
基金
美国国家科学基金会;
关键词
PHOTON DISSOCIATION SPECTRA; OXIDE CLUSTER CATIONS; VIBRATIONAL SPECTROSCOPY; C-H; TRANSITION-METAL; THEORETICAL INVESTIGATIONS; INFRARED-SPECTROSCOPY; ELECTRON-SPECTROSCOPY; COMPLEXES; ACTIVATION;
D O I
10.1063/1.5026899
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
La atom reaction with isoprene is carried out in a laser-vaporization molecular beam source. The reaction yields an adduct as the major product and C-C cleaved and dehydrogenated species as the minor ones. La(C5H8), La(C2H2), and La(C3H4) are characterized with mass-analyzed threshold ionization (MATI) spectroscopy and quantum chemical computations. The MATI spectra of all three species exhibit a strong origin band and several weak vibronic bands corresponding to La-ligand stretch and ligand-based bend excitations. La(C5H8) is a five-membered metallacycle, whereas La(C2H2) and La(C3H4) are three-membered rings. All three metallacycles prefer a doublet ground state with a La 6s(1)-based valence electron configuration and a singlet ion. The five-membered metallacycle is formed through La addition and isoprene isomerization, whereas the two three-membered rings are produced by La addition and insertion, hydrogen migration, and carbon-carbon bond cleavage. Published by AIP Publishing.
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页数:9
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